autosomal recessive woolly hair 3

Term ID

DOID:0111574

Synonyms

• ARWH3

Definition

A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KRT24 gene on chromosome 17q21.2. https://www.ncbi.nlm.nih.gov/pubmed/26160856

References

• OMIM:616760

Ontology

Human Disease   ( DOID:0111574 )